Welcome to Acta Agronomica Sinica,

Acta Agron Sin ›› 2010, Vol. 36 ›› Issue (2): 249-255.doi: 10.3724/SP.J.1006.2010.00249

• CROP GENETICS & BREEDING·GERMPLASM RESOURCES·MOLECULAR GENETICS • Previous Articles     Next Articles

 Identification and Analysis of TaWRKY34 Gene Induced by Wheat Powdery Mildew (Blumeria graminis f. sp. tritici)

QIN Wei1,2,ZHAO Guang-Yao2,QU Zhi-Cai1,*,ZHANG Li-Chao2,DUAN Jia-Lei2, LI Ai-Li2,JIA Ji-Zeng2,KONG Xiu-Ying2,*
  

  1. 1 College of Life Science, Qufu Normal University, Qufu 273165, China; 2 Key Laboratory of Crop Germplasm Resources and Utilization, Ministry of Agriculture / Institute of Crop Science, Chinese Academy of Agricultural Sciences / Key Facility for Crop Gene Resources and Genetic Improvement, Beijing 100081, China

  • Received:2009-05-06 Revised:2009-07-11 Online:2010-02-10 Published:2009-12-21

Abstract:

WRKY transcription factors play important roles in plant defense signaling network. However, little is known about the biological roles of WRKY proteins in wheat(Triticum aestivum L.). The objectives of this study were to screen WRKY transcription factor genes conferring resistance to powdery mildew (Blumeria graminis f. sp. tritici, Bgt) and disclose their function in wheat defense reaction. A WRKY transcription factor gene, TaWRKY34, was identified in response to Bgt by cDNA macroarray and semiquantitative RT-PCR from the wheat full-length cDNA libraries that were constructed in the authors’ earlier studies. This gene encodes 464 amino acid residues. TaWRKY34 was mapped onto short arms of chromosome 1B and 1D through blast search GrainGenes database and homemade full length cDNA library database of Aegilops tauschii. Further experiment indicated that TaWRKY34 also exists on chromosome 1AS through amplifying in Langdon D-genome disomic substitution lines and ChineseSpring nulli-tetrasomic lines with gene specific primers. Examining the subcellular localization of TaWARKY34, its coding region was fused to the 3’ end of green fluorescent protein (GFP). The GFP signal was detected only in the nucleus of onion epidermal cells to transiently express TaWRKY34-GFP, and the control-GFP protein distributed ubiquitously in both nuclei and cytoplasm. This suggests that TaWRKY34 is a nucleus-localized protein. Multiple sequence alignments of 57 WRKY domains from various species indicated that TaWRKY34 is closely related to WRKY transcription factors in response to pathogens in Arabidopsis thaliana (AtWRKY3, AtWRKY4 and AtWRKY33), Hordeum vulgare (HvWRKY42 and HvWRKY46), and Vitis vinifera (VvWRKY2) with identities ranging from 81.8% to 94.5%. Furthermore, TaWRKY34 has similar expression pattern with three sequences from A. thaliana, which was up-regulated at first and then down-regulated when inoculated with pathogens. The expression profiles of TaWRKY34 induced by powdery mildew fungus, salicylic acid and jasmonic acid were different between Pm16/Beijing 8377 near-isogenic lines (resistant to Bgt) and Beijing 837 (susceptible to Bgt). The results imply that TaWRKY34 is probably related to the resistance to powdery mildew in wheat.

Key words: Wheat, Blumeria graminis f. sp.tritici, WRKY transcription factor, Chromosome location, Expression pattern


[1] Eulgem T, Rushton P J, Robatzek S, Somssich I E. The WRKY superfamily of plant transcription factors. Trends Plant Sci, 2000, 5: 199-206

[2] Zhang Y J, Wang L J. The WRKY transcription factor superfamily: Its origin in eukaryotes and expansion in plants. BMC Evol Biol, 2005, 5: 1

[3] Eulgem T, Somssich I E. Networks of WRKY transcription factors in defense signaling. Curr Opin Plant Biol, 2007, 10: 366-371

[4] Kim K C, Lai Z B, Fan B F, Chen Z X. Arabidopsis WRKY38and WRKY62 transcription factors interact with histone deacetylase 19 in basal defense. Plant Cell, 2008, 20: 2357-2371

[5] Liu X Q, Bai X Q, Qian Q, Wang X J, Chen M S, Chu C C. OsWRKY03, a rice transcriptional activator that functions in defense signaling pathway upstream of OsNPR1. Cell Res, 2005, 15: 593-603

[6] Ryu H S, Han M, Lee S K, Cho J I, Ryoo N, Heu S, Lee Y H, Bhoo S H, Wang G L, Hahn T R, Jeon J S. A comprehensive expression analysis of the WRKY gene superfamily in rice plants during defense response. Plant Cell Rep, 2006, 25:836-847

[7] Cai M, Qiu D Y, Yuan T, Ding X H, Li H J, Duan L, Xu C G, Li X H, Wang S P. Identification of novel pathogen-responsive cis-elements and their binding proteins in the promoter of OsWRKY13, a gene regulating rice disease resistance. Plant Cell Environ, 2008, 31: 86-96

[8] Qiu D Y, Xiao J, Ding X H, Xiong M, Cai M, Cao Y, Li X H, Xu C G, Wang S P. OsWRKY13 mediates rice disease resistance by regulating defense-related genes in salicylate- and jasmonate-dependent signaling. Mol Plant Microbe Interact, 2007, 20: 492-499

[9] Zhang J, Peng Y L, Guo Z J. Constitutive expression of pathogen-inducible OsWRKY31 enhances disease resistance and affects root growth and auxin response in transgenic rice plants. Cell Res, 2008, 18: 508-521

[10] Shimono M, Sugano S, Nakayama A, Jiang C J, Ono K, Toki S, Takatsuji H. Rice WRKY45 plays a crucial role in benzothiadiazole-inducible blast resistance. Plant Cell, 2007, 19: 2064-2076

[11] Liu X Q, Bai X Q, Wang X J, Chu C C. OsWRKY71, a rice transcription factor, is involved in rice defense response. J Plant Physiol, 2007, 164: 969-979

[12] Wang H, Hao J, Chen X, Hao Z, Wang X, Lou Y, Peng Y, Guo Z. Overexpression of rice WRKY89 enhances ultraviolet B tolerance and disease resistance in rice plants. Plant Mol Biol, 2007, 65: 799-815

[13] Mangelsen E, Kilian J, Berendzen K W, Kolukisaoglu U H, Harter K, Jansson C, Wanke D. Phylogenetic and comparative gene expression analysis of barley (Hordeum vulgare) WRKY transcription factor family reveals putatively retained functions between monocots and dicots. BMC Genomics, 2008, 9: 194

[14] Shen Q H, Saijo Y, Mauch S, Biskup C, Bieri S, Keller B, Seki H, Ulker B, Somssich I E, Schulze-Lefert P. Nuclear activity of MLA immune receptors links isolate-specific and basal disease resistance responses. Science, 2007, 315: 1098-1103

[15] Bélanger R R, Benhamou N, Menzies J G. Cytological evidence of an active role of silicon in wheat resistance to powdery mildew (Blumeria graminis f. sp. tritici). Phytopathogy, 2003, 93: 402-412

[16] Bhuiyan N H, Liu W, Liu G S, Selvaraj G, Wei Y, King J. Transcriptional regulation of genes involved in the pathways of biosynthesis and supply of methyl units in response to powdery mildew attack and abiotic stresses in wheat. Plant Mol Biol, 2007, 64: 305-318

[17] Li A L, Wang M L, Zhou R H, Kong X Y, Hou N X, Wang W S, Jia J Z. Comparative analysis of early H2O2 accumulation in compatible and incompatible wheat-powdery mildew interactions. Plant Pathol, 2005, 54: 308-316

[18] AbuQamar S, Chen X, Dhawan R, Bluhm B, Salmeron J, Lam S, Dietrich R A, Mengiste T. Expression profiling and mutant analysis reveals complex regulatory networks involved in Arabidopsis response to Botrytis infection. Plant J, 2006, 48: 28-44

[19] Oh S K, Baek K H, Park J M, Yi S Y, Yu S H, Kamoun S, Choi D. Capsicum annuum WRKY protein CaWRKY1 is a negative regulator of pathogen defense. New Phytol, 2008, 177: 977-989

[20] Mzid R, Marchive C, Blancard D, Deluc L, Barrieua F, Corio-Costet M-F, Drirab N, Hamdi S, Lauvergeat V. Overexpression of VvWRKY2 in tobacco enhances broad resistance to necrotrophic fungal pathogens. Physiol Plant, 2007, 131: 434-447

[21] Dellagi A, Heilbronn J, Avrova A O, Montesano M, Palva E T, Stewart H E, Toth I K, Cooke D E L, Lyon G D, Birch P R J. A potato gene encoding a WRKY-like transcription factor is induced in interactions with Erwinia carotovora subsp. atroseptica and Phytophthora infestans and is coregulated with class I endochitinase expression. Mol Plant Microbe Interact,2000, 13: 1092-1101

[22] Chen C H, Chen Z X. Isolation and characterization of two pathogen-and salicylic acid-induced genes encoding WRKY DNA-binding proteins from tobacco. Plant Mol Biol, 2000, 42: 387-396

[23] Larkin M A, Blackshields G, Brown N P, Chenna R. McGettigan P A, McWilliam H, Valentin F, Wallace I M, Wilm A, Lopez R, Thompson J D, Gibson T G, Higgins D G. Clustal W and Clustal X version 2.0. Bioinformatics, 2007, 23: 2947-2948

[24] Clamp M, Cuff J, Searle S M, Barton G J. The Jalview Java alignment editor. Bioinformatics,2004, 20: 426-427

[25] Tamura K, Dudley J, Nei M, Kumar S. MEGA4: Molecular evolutionary genetics analysis (MEGA) software version 4.0. Mol Biol Evol, 2007, 24: 1596-1599

[26] Dong J X, Chen C H, Chen Z X. Expression profiles of the Arabidopsis WRKY gene superfamily during plant defense response. Plant Mol Biol, 2003, 51: 21-37

[27] Zheng Z Y, Qamar S A, Chen Z X, Mengiste T. Arabidopsis WRKY33 transcription factor is required for resistance to necrotrophic fungal pathogens. Plant J, 2006, 48: 592-605

[28] Loake G, Grant M. Salicylic acid in plant defense: The players and protagonists. Curr Opin in Plant Biol, 2007, 10: 466-472

[29] Panstruga R, Parker J E, Schulze-Lefert P. SnapShot: Plant immune response pathways. Cell, 2009, 136: 978.e1-3

[30] Schenk P M, Kazan K, Wilson I. Coordinated plant defense responses in Arabidopsis revealed by microarray analysis. Proc Natl Acad Sci USA, 2000, 97: 11655-11660

[31] Peng J Y, Deng X J, Huang J H, Jia S H, Miao X X, Huang Y P. Role of salicylic acid in tomato (Lycopersicon esculentum) plant defense against cotton bollworm, Helicoverpa armigera Hubner. Z Naturforsch C, 2004, 59: 856-862

[32] Lai Z H, Vinod K M, Zheng Z W, Fan B F, Chen Z X. Roles of Arabidopsis WRKY3 and WRKY4 transcription factors in plant responses to pathogens. BMC Plant Biol, 2008, 8: 68

[33] Robatzek S, Somssich, I E. Targets of AtWRKY6 regulation during plant senescence and pathogen defense. Genes Dev, 2002, 16: 1139-1149
[1] HU Wen-Jing, LI Dong-Sheng, YI Xin, ZHANG Chun-Mei, ZHANG Yong. Molecular mapping and validation of quantitative trait loci for spike-related traits and plant height in wheat [J]. Acta Agronomica Sinica, 2022, 48(6): 1346-1356.
[2] GUO Xing-Yu, LIU Peng-Zhao, WANG Rui, WANG Xiao-Li, LI Jun. Response of winter wheat yield, nitrogen use efficiency and soil nitrogen balance to rainfall types and nitrogen application rate in dryland [J]. Acta Agronomica Sinica, 2022, 48(5): 1262-1272.
[3] ZHU Zheng, WANG Tian-Xing-Zi, CHEN Yue, LIU Yu-Qing, YAN Gao-Wei, XU Shan, MA Jin-Jiao, DOU Shi-Juan, LI Li-Yun, LIU Guo-Zhen. Rice transcription factor WRKY68 plays a positive role in Xa21-mediated resistance to Xanthomonas oryzae pv. oryzae [J]. Acta Agronomica Sinica, 2022, 48(5): 1129-1140.
[4] LEI Xin-Hui, WAN Chen-Xi, TAO Jin-Cai, LENG Jia-Jun, WU Yi-Xin, WANG Jia-Le, WANG Peng-Ke, YANG Qing-Hua, FENG Bai-Li, GAO Jin-Feng. Effects of soaking seeds with MT and EBR on germination and seedling growth in buckwheat under salt stress [J]. Acta Agronomica Sinica, 2022, 48(5): 1210-1221.
[5] YUAN Da-Shuang, DENG Wan-Yu, WANG Zhen, PENG Qian, ZHANG Xiao-Li, YAO Meng-Nan, MIAO Wen-Jie, ZHU Dong-Ming, LI Jia-Na, LIANG Ying. Cloning and functional analysis of BnMAPK2 gene in Brassica napus [J]. Acta Agronomica Sinica, 2022, 48(4): 840-850.
[6] FU Mei-Yu, XIONG Hong-Chun, ZHOU Chun-Yun, GUO Hui-Jun, XIE Yong-Dun, ZHAO Lin-Shu, GU Jia-Yu, ZHAO Shi-Rong, DING Yu-Ping, XU Yan-Hao, LIU Lu-Xiang. Genetic analysis of wheat dwarf mutant je0098 and molecular mapping of dwarfing gene [J]. Acta Agronomica Sinica, 2022, 48(3): 580-589.
[7] HUANG Cheng, LIANG Xiao-Mei, DAI Cheng, WEN Jing, YI Bin, TU Jin-Xing, SHEN Jin-Xiong, FU Ting-Dong, MA Chao-Zhi. Genome wide analysis of BnAPs gene family in Brassica napus [J]. Acta Agronomica Sinica, 2022, 48(3): 597-607.
[8] FENG Jian-Chao, XU Bei-Ming, JIANG Xue-Li, HU Hai-Zhou, MA Ying, WANG Chen-Yang, WANG Yong-Hua, MA Dong-Yun. Distribution of phenolic compounds and antioxidant activities in layered grinding wheat flour and the regulation effect of nitrogen fertilizer application [J]. Acta Agronomica Sinica, 2022, 48(3): 704-715.
[9] LIU Yun-Jing, ZHENG Fei-Na, ZHANG Xiu, CHU Jin-Peng, YU Hai-Tao, DAI Xing-Long, HE Ming-Rong. Effects of wide range sowing on grain yield, quality, and nitrogen use of strong gluten wheat [J]. Acta Agronomica Sinica, 2022, 48(3): 716-725.
[10] YAN Yan, ZHANG Yu-Shi, LIU Chu-Rong, REN Dan-Yang, LIU Hong-Run, LIU Xue-Qing, ZHANG Ming-Cai, LI Zhao-Hu. Variety matching and resource use efficiency of the winter wheat-summer maize “double late” cropping system [J]. Acta Agronomica Sinica, 2022, 48(2): 423-436.
[11] WANG Yang-Yang, HE Li, REN De-Chao, DUAN Jian-Zhao, HU Xin, LIU Wan-Dai, GU Tian-Cai, WANG Yong-Hua, FENG Wei. Evaluations of winter wheat late frost damage under different water based on principal component-cluster analysis [J]. Acta Agronomica Sinica, 2022, 48(2): 448-462.
[12] CHEN Xin-Yi, SONG Yu-Hang, ZHANG Meng-Han, LI Xiao-Yan, LI Hua, WANG Yue-Xia, QI Xue-Li. Effects of water deficit on physiology and biochemistry of seedlings of different wheat varieties and the alleviation effect of exogenous application of 5-aminolevulinic acid [J]. Acta Agronomica Sinica, 2022, 48(2): 478-487.
[13] XU Long-Long, YIN Wen, HU Fa-Long, FAN Hong, FAN Zhi-Long, ZHAO Cai, YU Ai-Zhong, CHAI Qiang. Effect of water and nitrogen reduction on main photosynthetic physiological parameters of film-mulched maize no-tillage rotation wheat [J]. Acta Agronomica Sinica, 2022, 48(2): 437-447.
[14] MA Bo-Wen, LI Qing, CAI Jian, ZHOU Qin, HUANG Mei, DAI Ting-Bo, WANG Xiao, JIANG Dong. Physiological mechanisms of pre-anthesis waterlogging priming on waterlogging stress tolerance under post-anthesis in wheat [J]. Acta Agronomica Sinica, 2022, 48(1): 151-164.
[15] JIAN Hong-Ju, SHANG Li-Na, JIN Zhong-Hui, DING Yi, LI Yan, WANG Ji-Chun, HU Bai-Geng, Vadim Khassanov, LYU Dian-Qiu. Genome-wide identification and characterization of PIF genes and their response to high temperature stress in potato [J]. Acta Agronomica Sinica, 2022, 48(1): 86-98.
Viewed
Full text


Abstract

Cited

  Shared   
  Discussed   
No Suggested Reading articles found!